<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE247266" accession="SRP470691">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP470691</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA1037015</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE247266</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Transcriptome analysis reveals the mechanism of bovine lactoferrin against lipopolysaccharide-induced acute lung injury</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Lactoferrin (LF) is an iron-binding multifunctional cationic glycoprotein secreted by exocrine glands and neutrophils in mammals. In this study, we created a mouse model of lipopolysaccharide (LPS)-induced acute lung injury and explored the anti-inflammatory effect and mechanism of bovine lactoferrin (bLF) in acute lung injury using the RNA sequencing (RNA-seq) technology and transcriptome analysis. Overall design: A total of 24 mice were randomly divided into 4 groups (n = 6): control, LPS (lipopolysaccharide, 50 µL, 1 µg/µL), bLF (bovine lactoferrin, 200 mg/kg/day), and treatment (LPS+bLF). After 14 days of modeling, lung tissues of 12 mice from the control, LPS, bLF, and LPS+bLF groups (n = 3) were used for RNA-seq analysis. mRNA library construction and transcriptome sequencing (RNA-seq) were performed by the BGI Institute of Life Sciences (Shenzhen, China).</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE247266</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>38578368</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
